Canonical Allele Identifier: CA649016702

Gene: GNRHR

Linked Data

• COSMIC: COSN16481535

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740252_67740253insG , CM000666.2:g.67740252_67740253insG	GRCh38
NC_000004.11:g.68605970_68605971insG , CM000666.1:g.68605970_68605971insG	GRCh37
NC_000004.10:g.68288565_68288566insG	NCBI36
NG_009293.1:g.20834_20835insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.*227_*228insC MANE Select	ENSP00000226413.5:n.*227_*228insC
ENST00000226413.4:c.*227_*228insC	ENSP00000226413.4:n.*227_*228insC
NM_000406.2:c.*227_*228insC	NP_000397.1:n.*227_*228insC
NM_001012763.1:c.*336_*337insC	NP_001012781.1:n.*336_*337insC
NM_000406.3:c.*227_*228insC MANE Select	NP_000397.1:n.*227_*228insC
NM_001012763.2:c.*336_*337insC	NP_001012781.1:n.*336_*337insC